Total synthesis of biologically active metabolites of arachidonic acid. The two 8-hydroxy-11,12(S,S)-epoxyeicosa-5,14(Z),9(E)-trienoic acids.
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (45) , 5119-5122
- https://doi.org/10.1016/s0040-4039(01)81539-2
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Stereochemistry of the lipoxygenase-catalyzed allylic hydroperoxide→oxiranylcarbinol rearrangementsTetrahedron Letters, 1983
- New synthetic routes to leukotrienes and other arachidonate derived epoxy eicosatetraenoic acids (epete's). Exclusion of the hydroxy epoxide pathway for leukotriene biosynthesisTetrahedron Letters, 1983
- Total synthesis of 12-()-10-hydroxy--11,12-epoxyeicosa-5,9,14-()-trienoic acids, metabolites of arachidonic acid in mammalian blood plateletsTetrahedron Letters, 1983
- A Stereocontrolled and effective synthesis of leukotriene B (Tetrahedron Letters, 1981
- Leukotriene B. Total synthesis and assignment of stereochemistryJournal of the American Chemical Society, 1980
- A new reaction of unsaturated fatty acid hydroperoxides: Formation of 11‐hydroxy‐12,13‐epoxy‐9‐octadecenoic acid from 13‐hydroperoxy‐9,11‐octadecadienoic acidLipids, 1973